참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Quinone | HCID 4650 | — |
| 반응물 | Sodium Iodide | HCID 5238 | — |
| 반응물 | 1,2-Bis(dibromomethyl)benzene | HCID 83234 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 6,13-Pentacenequinone | HCID 76415 | 91% |
반응 단계
To a clear solution of α,α,α′,α′-tetrabromo-o-xylene (30.5 g, 0.073 mol) in DMF (100 mL) was added benzoquinone (3.125 g, 0.03 mol) and sodium iodide (27.25 g, 0.18 mol). The resulting brown suspension was heated and stirred at 120° C. overnight. After cooling to RT, the yellow solids were filtered via vacuum filtration. The yellow solids were washed with water, saturated sodium bisulfite solution and dried to yield the product (8.1 g, 91%). 1H NMR (500 MHz, CDCl3): δ 8.96 (s, 4H), 8.14 (m, 4H), 7.72 (m, 4H). 13C NMR (125.68 MHz, CDCl3): δ 183.2, 135.47, 130.80, 130.30, 129.98, 129.66. m/z: 308 [M+].
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US08513466B2 |
|---|
| 출처 데이터셋 | uspto-grants-2013_08 |
|---|
| ORD ID | ord-dd94acd8cb7347b59690211fdb09a179 |
|---|
| 출처 메모 | uspto-grants-2013_08 |
|---|